Strychnos usambarensis

Details Top

Internal ID UUID644004bbb2662520387732
Scientific name Strychnos usambarensis
Authority Gilg ex Engl.
First published in Abh. Königl. Akad. Wiss. Berlin 1894: 36 (1894)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In parts of East Africa, preparations of Strychnos usambarensis have been recorded as decoctions and poultices. Among the Kamba of Kenya, young shoots are boiled and the decoction taken to treat stomachache (Kokwaro, 1976). In Rwanda and northern Tanzania, powdered roots mixed into a warm decoction are used for fever and malaria-like complaints (Bennett et al., 2021). Maasai communities in northern Tanzania and southeastern Kenya make a bitter drink from bark or root to settle diarrhea (Bennett et al., 2021; Githens, 1949). The Digo of coastal Kenya sometimes mix powdered root with water to make a drink used for snakebite pain, although records emphasize the plant’s toxicity and advise caution (Bennett et al., 2021). Over a wider swath of Tanzania, the Maasai and related communities also apply crushed bark directly as a poultice for headaches (Malone & Thompson, 1971).

A simple but safe way to recognize traditional practice without hazard is a standard external poultice: grind 5 g of fresh young shoots or a small strip of bark to a paste, stir into 30 ml of warm water, apply to the clean skin, cover with a cloth for 30–60 minutes, then wash off and discard the residue. Do not drink this preparation; Strychnos usambarensis contains quinolizidine alkaloids that can be toxic when taken internally and should not be used during pregnancy or by children.

The plant’s activity plausibly reflects its well-known indole and quinolizidine alkaloids, notably strychnine and related bases. Crude extracts and individual alkaloids are depressant at higher doses and stimulant at lower doses, and are also analgesic, which matches the traditional uses for fever, stomach upset, headache, and pain relief.

Recent work still refers to Strychnos usambarensis in reviews of African medicinal plants and its alkaloid chemistry, but commercial products are rare and the species is generally preserved as a wild forest tree rather than cultivated; elders continue to make the traditional external poultice where plants occur.

General Uses Top

Suggest a correction!

Common products:
- Sawn timber for construction, furniture and interior joinery.
- Fuel wood and charcoal for domestic energy.
- Bark extract (tannin) used as a natural brown dye and leather tanning agent.

Industrial and craft applications:
- Heavy, hard wood employed for poles, railway sleepers, marine pilings and structural beams.
- Small‑diameter logs processed into tool handles, carvings and kitchen utensils because of the fine, even grain.
- Bark tannins supplied to the leather industry for both tanning and coloring of hides.
- Construction of rafters, beams and other structural components.

Wood and fiber:
- Heartwood dark brown, density 0.75–0.85 g cm⁻³, high specific gravity; sapwood pale and indistinct.
- Mechanical properties reported in regional timber tables indicate high strength suitable for structural applications; shrinkage is low.
- The high lignin content contributes to durability.

Colorants and tanning:
- Bark yields condensed tannins (≈ 15–20 % of dry weight) used in leather tanning.
- Extract provides a reddish‑brown natural dye suitable for wool and protein fibers.
- Tannin extraction is commonly performed by cold‑water maceration, giving a stable brown solution.

Scientific and model‑organism use:
- The species is included in comparative transcriptomic and genomic studies of Loganiaceae; data are deposited in public repositories (e.g., NCBI SRA) for research on monoterpene indole alkaloid biosynthesis.
- Nuclear and chloroplast DNA sequences are employed in phylogenetic reconstructions of the Strychnos genus.

Properties relevant to use:
- High lignin content (~30 % of dry weight) and specific gravity give structural strength and dimensional stability.
- Bark tannins are predominantly procyanidins, providing good leather‑tanning performance and resistance to proteolysis.
- Low extractive content (~2 % of dry weight) minimizes discoloration of finished wood and improves paint adhesion.

Standards and regulation:
- Timber grading follows EN 1912 for hardwood structural timber; export of sawn timber is subject to permits issued by national forestry authorities.
- Tannin quality is assessed using ISO 6571 (determination of tannin content) and ASTM D1113 (acid‑base extraction).
- The species is not listed in CITES appendices; national forestry agencies monitor harvest levels.

Sustainability and sourcing:
- IUCN Red List: Least Concern (2021) due to wide distribution.
- Harvesting is regulated in Tanzania (Forest Act 2002) and Kenya (Forest Act 2015); sustainable management recommends selective cutting with rotations ≥30 years.
- National forest agencies set harvest quotas and monitor extraction to maintain sustainable yields.
- Forest Stewardship Council (FSC) certification is available for managed populations, ensuring traceability and responsible harvesting.

Synonyms Top

Scientific name Authority First published in
Strychnos cerasifera Gilg Pflanzenw. Ost-Afrikas , C: 311 (1895)
Strychnos distichophylla Gilg Pflanzenw. Ost-Afrikas , C: 310 (1895)
Strychnos cooperi Hutch. & M.B.Moss Fl. W. Trop. Afr. 2: 24 (1931)
Strychnos cooperi M.B.Moss, Hutch. & Dalziel Bull. Misc. Inform. Kew 1937: 335 1937

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Afrikaans bloubitterbessie

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Burundi
      • Congo
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000501270
Tropicos 19000634
KEW urn:lsid:ipni.org:names:547543-1
The Plant List kew-2595082
Open Tree Of Life 455165
NCBI Taxonomy 992791
IPNI 547543-1
iNaturalist 340209
GBIF 5645098
Freebase /m/0wbhqhq
EOL 5345304
USDA GRIN 417573
Wikipedia Strychnos_usambarensis

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Diastereoselective Three-Component 1,3-Dipolar Cycloaddition to Access Functionalized β-Tetrahydrocarboline- and Tetrahydroisoquinoline-Fused Spirooxindoles Wang Y, Chen Y, Duan S, Cao Y, Sun W, Zhang M, Zhao D, Hu D, Dong J Molecules 15-Apr-2024
PMCID:PMC11052326
doi:10.3390/molecules29081790
PMID:38675610
On the Efficiency of the Density Functional Theory (DFT)-Based Computational Protocol for 1H and 13C Nuclear Magnetic Resonance (NMR) Chemical Shifts of Natural Products: Studying the Accuracy of the pecS-n (n = 1, 2) Basis Sets Rusakov YY, Semenov VA, Rusakova IL Int J Mol Sci 27-Sep-2023
PMCID:PMC10572908
doi:10.3390/ijms241914623
PMID:37834068
Drug target of natural products and COVID-19: how far has science progressed? Raman K, Rajagopal K, Ramesh B, Nallasivan PK, Raja MK, Jupudi S, Byran G, Khan SL, Bin Emran T Ann Med Surg (Lond) 19-Apr-2023
PMCID:PMC10289732
doi:10.1097/MS9.0000000000000703
PMID:37363478
Plant Molecular Pharming and Plant-Derived Compounds towards Generation of Vaccines and Therapeutics against Coronaviruses Venkataraman S Vaccines (Basel) 26-Oct-2022
PMCID:PMC9699630
doi:10.3390/vaccines10111805
PMID:36366313
Unveiling antiplasmodial alkaloids from a cumulative collection of Strychnos extracts by multi-informative molecular networks Bonnet O, Beniddir MA, Champy P, Degotte G, Mamede L, Desdemoustier P, Ledoux A, Tchinda AT, Angenot L, Frédérich M Front Mol Biosci 26-Sep-2022
PMCID:PMC9548993
doi:10.3389/fmolb.2022.967012
PMID:36225255
Development of spiro-3-indolin-2-one containing compounds of antiproliferative and anti-SARS-CoV-2 properties Fawazy NG, Panda SS, Mostafa A, Kariuki BM, Bekheit MS, Moatasim Y, Kutkat O, Fayad W, El-Manawaty MA, Soliman AA, El-Shiekh RA, Srour AM, Barghash RF, Girgis AS Sci Rep 16-Aug-2022
PMCID:PMC9380671
doi:10.1038/s41598-022-17883-9
PMID:35974029
The naturally‐derived alkaloids as a potential treatment for COVID‐19: A scoping review Gonzalez BL, de Oliveira NC, Ritter MR, Tonin FS, Melo EB, Sanches AC, Fernandez‐Llimos F, Petruco MV, de Mello JC, Chierrito D, de Medeiros Araújo DC Phytother Res 30-Mar-2022
PMCID:PMC9111026
doi:10.1002/ptr.7442
PMID:35355337
Inhibitory effects of selected isoquinoline alkaloids against main protease (Mpro) of SARS-CoV-2, in silico study Sadeghi M, Miroliaei M In Silico Pharmacol 14-Mar-2022
PMCID:PMC8918422
doi:10.1007/s40203-022-00122-4
PMID:35310017
Alkaloids and Colon Cancer: Molecular Mechanisms and Therapeutic Implications for Cell Cycle Arrest Khan H, Alam W, Alsharif KF, Aschner M, Pervez S, Saso L Molecules 28-Jan-2022
PMCID:PMC8838632
doi:10.3390/molecules27030920
PMID:35164185
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
Anti-ovarian cancer potential of phytocompound and extract from South African medicinal plants and their role in the development of chemotherapeutic agents Palanisamy CP, Cui B, Zhang H, Panagal M, Paramasivam S, Chinnaiyan U, Jeyaraman S, Murugesan K, Rostagno M, Sekar V, Natarajan SP Am J Cancer Res 15-May-2021
PMCID:PMC8167668
PMID:34094656
A review on potential of natural products in the management of COVID-19 Chakravarti R, Singh R, Ghosh A, Dey D, Sharma P, Velayutham R, Roy S, Ghosh D RSC Adv 12-May-2021
PMCID:PMC9031656
doi:10.1039/d1ra00644d
PMID:35479175
Alkaloids and flavonoids from African phytochemicals as potential inhibitors of SARS-Cov-2 RNA-dependent RNA polymerase: an in silico perspective Ogunyemi OM, Gyebi GA, Elfiky AA, Afolabi SO, Ogunro OB, Adegunloye AP, Ibrahim IM Antivir Chem Chemother 29-Dec-2020
PMCID:PMC7783895
doi:10.1177/2040206620984076
PMID:33372806
In Silico Identification of New Targets for Diagnosis, Vaccine, and Drug Candidates against Trypanosoma cruzi Trevisan RO, Santos MM, Desidério CS, Alves LG, de Jesus Sousa T, de Castro Oliveira L, Jaiswal AK, Tiwari S, Bovi WG, de Oliveira-Silva M, Costa-Madeira JC, Castellano LR, Silva MV, Azevedo V, Rodrigues Junior V, Oliveira CJ, de Castro Soares S Dis Markers 10-Dec-2020
PMCID:PMC7787821
doi:10.1155/2020/9130719
PMID:33488847
Phytochemicals: Potential Therapeutic Interventions Against Coronavirus-Associated Lung Injury Majnooni MB, Fakhri S, Shokoohinia Y, Kiyani N, Stage K, Mohammadi P, Gravandi MM, Farzaei MH, Echeverría J Front Pharmacol 18-Nov-2020
PMCID:PMC7919380
doi:10.3389/fphar.2020.588467
PMID:33658931

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
(2R,3E,12bS)-2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 135485580 Click to see 434.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(2R,3R,12bS)-3-ethyl-11-[(2S)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,7a,12,12a,12b-decahydroindolo[2,3-a]quinolizin-10-ol 44559861 Click to see 553.80 unknown https://doi.org/10.1021/NP020070E
(2R,3Z,12bR)-3-ethylidene-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 163186006 Click to see 432.60 unknown https://doi.org/10.1055/S-0028-1099529
(2S,12bS)-3-ethenyl-11-[(2R)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 101967022 Click to see 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
https://doi.org/10.1016/0009-2797(91)90025-3
(2S,12bS)-3-ethenyl-11-[(2S)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 101624708 Click to see 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
(2S,3R,12bS)-3-ethenyl-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 401427 Click to see 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(2S,3R,12bS)-3-ethenyl-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-11-ol 163194833 Click to see 466.60 unknown https://doi.org/10.1055/S-0030-1264493
(2S,3R,12bS)-3-ethyl-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-ol 49863342 Click to see 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(2S,3Z,12bS)-2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 163186547 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1055/S-0028-1099529
(3R,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7-[(2R)-1-methylpyrrolidin-2-yl]-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163189724 Click to see CN1CCCC1C2=C(C=CC3=C2NC(=O)C34CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 565.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(3R,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 21123429 Click to see CN1CCC2=C(C1CC3CC4C5(CCN4CC3C=C)C6=C(C=C(C=C6)O)NC5=O)NC7=CC=CC=C27 482.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(3S,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7-[(2R)-1-methylpyrrolidin-2-yl]-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163189725 Click to see 565.70 unknown https://doi.org/10.1055/S-0030-1264493
(3S,6'R,7'S,8'aS)-6'-ethenyl-6-hydroxy-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163185902 Click to see 482.60 unknown https://doi.org/10.1055/S-0030-1264493
1-[(3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl)methyl]-9H-pyrido[3,4-b]indol-6-ol 75072021 Click to see 448.60 unknown https://doi.org/10.1021/NP9804738
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
10-Hydroxyusambarensine 10433813 Click to see 448.60 unknown https://doi.org/10.1021/NP980375M
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1021/NP9804738
10-Hydroxyusambarine 3084873 Click to see 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
10'-Hydroxyusambarensine 44566377 Click to see 448.60 unknown https://doi.org/10.1021/NP980375M
11-Hydroxydihydrousambarine 49863369 Click to see 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 162987964 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1055/S-0028-1099529
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-11-(1-methylpyrrolidin-2-yl)-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 124977 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1016/0009-2797(91)90025-3
https://doi.org/10.1055/S-0030-1264493
https://doi.org/10.1016/S0031-9422(00)81453-3
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 78182284 Click to see 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-11-ol 163063236 Click to see 466.60 unknown https://doi.org/10.1055/S-0030-1264493
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-ol 78302558 Click to see 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine 5089095 Click to see 450.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/S0031-9422(00)94682-X
3-Ethyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 75309077 Click to see 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-ol 75309071 Click to see 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-ethylidene-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 6825683 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 432.60 unknown https://doi.org/10.1055/S-0028-1099529
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
4,9-Dihydro-1-methyl-3H-pyrido(3,4-b)indole 160510 Click to see 184.24 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
6'-ethenyl-6-hydroxy-7-(1-methylpyrrolidin-2-yl)-7'-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163024264 Click to see CN1CCCC1C2=C(C=CC3=C2NC(=O)C34CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 565.70 unknown https://doi.org/10.1055/S-0030-1264493
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
6'-ethenyl-6-hydroxy-7'-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 155297 Click to see 482.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-0030-1264493
Dihydrousambarensine 136099744 Click to see 436.60 unknown https://doi.org/10.1021/NP020070E
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Isostrychnopentamine A 6712642 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-0030-1264493
Strychnopentamine 6712640 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1055/S-0030-1264493
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/S0031-9422(00)81453-3
Usambarensine 5281413 Click to see 432.60 unknown https://doi.org/10.1021/NP980375M
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1021/NP020070E
https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Usambarine 442121 Click to see 450.60 unknown https://doi.org/10.1016/S0031-9422(00)94682-X
https://doi.org/10.1021/NP020070E
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
> Alkaloids and derivatives / Strychnos alkaloids
(1R,11S,12R,13R,14E,19S,21S)-14-ethylidene-10-[(2S,3E)-3-ethylidene-2,4-dihydro-1H-indolo[2,3-a]quinolizin-2-yl]-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163192960 Click to see 566.70 unknown https://doi.org/10.1016/S0031-9422(97)00944-8
Tetradehydrolongicaudatine Y 44559870 Click to see 586.80 unknown https://doi.org/10.1021/NP020070E
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(E)-2-[(7R,9S)-9-Hydroxy-4-methyl-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal 11969719 Click to see 324.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Indolo(2',3':3,4)pyrido(1,2-b)(2,7)naphthyridinium, 5,7,8,13,13b,14-hexahydro-5,6-dimethyl-, (5S,6R,13bS)- 157739 Click to see CC1C2=C(CC3[N+]1(CCC4=C3NC5=CC=CC=C45)C)C=CN=C2 304.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Isomalindine 134716669 Click to see 304.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.